Prsandoz® ABIRATERONE

PRODUCT MONOGRAPH PrSANDOZ® ABIRATERONE Abiraterone Acetate Tablets, Mfr. Std. 250 mg tablets Androgen Biosynthesis Inhibitor Sandoz Canada Inc. Date of Revision: 110 Rue de Lauzon December 11, 2019 Boucherville, Quebec J4B 1E6 Submission Control No: 234103 Sandoz Abiraterone Page 1 of 52 Table of Contents PART I: HEALTH PROFESSIONAL INFORMATION ........................................................ 3 SUMMARY PRODUCT INFORMATION........................................................................ 3 INDICATIONS AND CLINICAL USE ............................................................................. 3 CONTRAINDICATIONS ................................................................................................. 34 WARNINGS AND PRECAUTIONS ................................................................................. 4 ADVERSE REACTIONS ................................................................................................... 8 DRUG INTERACTIONS ................................................................................................. 17 DOSAGE AND ADMINISTRATION ............................................................................. 19 OVERDOSAGE ................................................................................................................ 20 ACTION AND CLINICAL PHARMACOLOGY ............................................................ 20 STORAGE AND STABILITY ......................................................................................... 24 SPECIAL HANDLING INSTRUCTIONS ....................................................................... 24 DOSAGE FORMS, COMPOSITION AND PACKAGING............................................. 24 PART II: SCIENTIFIC INFORMATION .............................................................................. 25 PHARMACEUTICAL INFORMATION ......................................................................... 25 CLINICAL TRIALS ......................................................................................................... 26 DETAILED PHARMACOLOGY .................................................................................... 47 TOXICOLOGY ................................................................................................................. 47 REFERENCES .................................................................................................................. 49 PART III: CONSUMER INFORMATION ............................................................................. 50 Sandoz Abiraterone Page 2 of 52 PrSandoz Abiraterone Abiraterone acetate tablets, Mfr. Std 250 mg tablets Androgen Biosynthesis Inhibitor PART I: HEALTH PROFESSIONAL INFORMATION SUMMARY PRODUCT INFORMATION Route of Dosage Form / Clinically Relevant Nonmedicinal Administration Strength Ingredients Oral Tablet Lactose monohydrate 250 mg For a complete listing see DOSAGE FORMS, COMPOSITION AND PACKAGING section. INDICATIONS AND CLINICAL USE Sandoz Abiraterone is indicated in combination with prednisone for the treatment of metastatic prostate cancer (castration-resistant prostate cancer, mCRPC) in patients who: are asymptomatic or mildly symptomatic after failure of androgen deprivation therapy have received prior chemotherapy containing docetaxel after failure of androgen deprivation therapy Sandoz Abiraterone is also indicated in combination with prednisone and androgen deprivation therapy (ADT) for the treatment of patients with newly diagnosed hormone-sensitive high-risk metastatic prostate cancer who may have received up to 3 months of prior ADT. Geriatrics (≥ 65 years of age): In the Phase 3 studies of abiraterone acetate, 70% of patients were 65 years and over, and 27% of patients were 75 years and over. No overall differences in safety or effectiveness were observed between these elderly patients and younger patients (see WARNINGS AND PRECAUTIONS, Special Populations, Geriatrics). Pediatrics: Abiraterone acetate has not been studied in children. CONTRAINDICATIONS Sandoz Abiraterone Page 3 of 52 . Patients who are hypersensitive to this drug or to any ingredient in the formulation or component of the container. For a complete listing, see the DOSAGE FORMS, COMPOSITION AND PACKAGING section of the Product Monograph. Women who are or may potentially be pregnant. WARNINGS AND PRECAUTIONS Serious Warnings and Precautions Sandoz Abiraterone may cause hypertension, hypokalemia and fluid retention due to mineralocorticoid excess (see WARNINGS AND PRECAUTIONS, Cardiovascular) Sandoz Abiraterone should be used with caution in patients with a history of cardiovascular disease (for specific conditions see WARNINGS AND PRECAUTIONS, Cardiovascular) Patients with severe and moderate hepatic impairment should not receive Sandoz Abiraterone (see WARNINGS AND PRECAUTIONS, Special Populations, Patients with Hepatic Impairment) Hepatotoxicity, including fatal cases has been observed (see WARNINGS AND PRECAUTIONS, Hepatic) General Gonadotropin releasing hormone (GnRH) agonists must be taken during treatment with Sandoz Abiraterone or patients must have been previously treated with orchiectomy. Sandoz Abiraterone must be taken on an empty stomach. No solid or liquid food should be consumed for at least two hours before the dose of Sandoz Abiraterone is taken and for at least one hour after the dose of Sandoz Abiraterone is taken. Abiraterone Cmax and AUC0-∞ (exposure) were increased up to 17- and 10-fold higher, respectively, when a single dose of abiraterone acetate was administered with a meal compared to a fasted state. The safety of these increased exposures when multiple doses of abiraterone acetate are taken with food has not been assessed (see DRUG INTERACTIONS Drug-Food Interactions, DOSAGE AND ADMINISTRATION, and ACTION AND CLINICAL PHARMACOLOGY). Reproductive Toxicology In fertility studies in both male and female rats, abiraterone acetate reduced fertility, which was completely reversible in 4 to 16 weeks after abiraterone acetate was stopped. In a developmental toxicity study in the rat, abiraterone acetate affected pregnancy including reduced fetal weight Sandoz Abiraterone Page 4 of 52 and survival. Effects on the external genitalia were observed though abiraterone acetate was not teratogenic. In these fertility and developmental toxicity studies performed in the rat, all effects were related to the pharmacological activity of abiraterone (see TOXICOLOGY, Reproductive Toxicology). Carcinogenesis and Mutagenesis Abiraterone acetate was not carcinogenic in a 6-month study in the transgenic (Tg.rasH2) mouse. In a 24-month carcinogenicity study in the rat, abiraterone acetate increased the incidence of interstitial cell neoplasms in the testes. This finding is considered related to the pharmacological action of abiraterone. The clinical relevance of this finding is not known. Abiraterone acetate was not carcinogenic in female rats (see TOXICOLOGY, Carcinogenesis and Genotoxicity). Abiraterone acetate and abiraterone were devoid of genotoxic potential in the standard panel of in vitro and in vivo genotoxicity tests (see Product TOXICOLOGY, Carcinogenesis and Genotoxicity). Cardiovascular Sandoz Abiraterone should be used with caution in patients with a history of cardiovascular disease. The safety of abiraterone acetate in patients with myocardial infarction, or arterial thrombotic events in the past 6 months, severe or unstable angina, or left ventricular ejection fraction (LVEF) < 50% or New York Heart Association Class III or IV heart failure (in patients with mCRPC with prior treatment with docetaxel) or NYHA Class II to IV heart failure (in patients with asymptomatic or mildly symptomatic mCRPC, or newly diagnosed high-risk metastatic prostate cancer) has not been established because these patients were excluded from the pivotal studies. Hypertension, Hypokalemia and Fluid Retention Due to Mineralocorticoid Excess Before treatment with Sandoz Abiraterone, hypertension must be controlled, and hypokalemia must be corrected. Abiraterone acetate may cause hypertension, hypokalemia and fluid retention (see ADVERSE REACTIONS) as a consequence of increased mineralocorticoid levels resulting from CYP17 inhibition (see ACTION AND CLINICAL PHARMACOLOGY, Mechanism of Action). Co-administration of a corticosteroid suppresses adrenocorticotropic hormone (ACTH) drive, resulting in a reduction in the incidence and severity of these adverse reactions. Caution is required in treating patients whose underlying medical conditions might be compromised by potential increases in blood pressure, hypokalemia or fluid retention, e.g., those with heart failure, recent myocardial infarction or ventricular arrhythmia. In post marketing experience, QT prolongation and Torsades de Pointes have been observed in patients who develop hypokalemia or have underlying cardiovascular conditions while taking abiraterone acetate Blood pressure, serum potassium and fluid retention should be monitored at least monthly (see Monitoring and Laboratory Tests). Corticosteroid Withdrawal and Coverage of Stress Situations Caution is advised if patients need to be withdrawn from prednisone. Monitoring for Sandoz Abiraterone Page 5 of 52 adrenocortical insufficiency should occur. If Abiraterone acetate is continued after corticosteroids are withdrawn, patients should be monitored for symptoms of mineralocorticoid excess. In patients on prednisone who are subjected to unusual stress (e.g., surgery, trauma or severe infections), increased dosage of a corticosteroid may

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